Načítá se...

Fetal hemoglobin silencing in humans

Interruption of the normal fetal-to-adult transition of hemoglobin expression should largely ameliorate sickle cell and beta-thalassemia syndromes. Achievement of this clinical goal requires a robust understanding of gamma-globin gene and protein silencing during human development. For this purpose,...

Celý popis

Uloženo v:
Podrobná bibliografie
Hlavní autoři: Oneal, Patricia A., Gantt, Nicole M., Schwartz, Joseph D., Bhanu, Natarajan V., Lee, Y. Terry, Moroney, John W., Reed, Christopher H., Schechter, Alan N., Luban, Naomi L. C., Miller, Jeffery L.
Médium: Artigo
Jazyk:Inglês
Vydáno: The American Society of Hematology 2006
Témata:
On-line přístup:https://ncbi.nlm.nih.gov/pmc/articles/PMC1895549/
https://ncbi.nlm.nih.gov/pubmed/16735596
https://ncbi.nlm.nih.govhttp://dx.doi.org/10.1182/blood-2006-04-015859
Tagy: Přidat tag
Žádné tagy, Buďte první, kdo otaguje tento záznam!